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肿瘤-宿主相互作用及药物反应的全身亚细胞多色实时成像

Whole-body subcellular multicolor imaging of tumor-host interaction and drug response in real time.

作者信息

Yang Meng, Jiang Ping, Hoffman Robert M

机构信息

AntiCancer, Inc, San Diego, California 92111, USA.

出版信息

Cancer Res. 2007 Jun 1;67(11):5195-200. doi: 10.1158/0008-5472.CAN-06-4590.

Abstract

To noninvasively image cancer cell/stromal cell interaction in the tumor microenvironment and drug response at the cellular level in live animals in real time, we developed a new imageable three-color animal model. The model consists of green fluorescent protein (GFP)-expressing mice transplanted with dual-color cancer cells labeled with GFP in the nucleus and red fluorescent protein in the cytoplasm. The Olympus IV100 Laser Scanning Microscope, with ultra-narrow microscope objectives ("stick objectives"), is used for three-color whole-body imaging of the two-color cancer cells interacting with the GFP-expressing stromal cells. In this model, drug response of both cancer and stromal cells in the intact live animal is also imaged in real time. Various in vivo phenomena of tumor-host interaction and cellular dynamics were imaged, including mitotic and apoptotic tumor cells, stromal cells interacting with the tumor cells, tumor vasculature, and tumor blood flow. This new model system enables the first cellular and subcellular images of unperturbed tumors in the live intact animal. New visible real-time targets for novel anticancer agents are provided in this model, including the color-coded interacting cancer and stromal cells, tumor vasculature, and blood flow. This imageable model should lead to many new insights of in vivo cancer cell biology and to novel drug discovery.

摘要

为了在活体动物中实时、无创地在细胞水平对肿瘤微环境中的癌细胞/基质细胞相互作用及药物反应进行成像,我们开发了一种新的可成像三色动物模型。该模型由移植了双色癌细胞的绿色荧光蛋白(GFP)表达小鼠组成,双色癌细胞的细胞核标记有GFP,细胞质标记有红色荧光蛋白。配备超窄显微镜物镜(“棒状物镜”)的奥林巴斯IV100激光扫描显微镜用于对与表达GFP的基质细胞相互作用的双色癌细胞进行三色全身成像。在该模型中,还可实时对完整活体动物中癌细胞和基质细胞的药物反应进行成像。对肿瘤-宿主相互作用和细胞动态的各种体内现象进行了成像,包括有丝分裂和凋亡的肿瘤细胞、与肿瘤细胞相互作用的基质细胞、肿瘤脉管系统和肿瘤血流。这个新的模型系统能够首次在完整的活体动物中获取未受干扰肿瘤的细胞和亚细胞图像。该模型提供了新型抗癌药物新的可见实时靶点,包括颜色编码的相互作用癌细胞和基质细胞、肿瘤脉管系统及血流。这种可成像模型应能为体内癌细胞生物学带来许多新见解,并推动新型药物的发现。

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